Lancet. 2021 May 1;397(10285):1637-1645. doi: 10.1016/S0140-6736(21)00676-0.
BACKGROUND: In this study, we aimed to evaluate the effects of tocilizumab in adult patients admitted to hospital with COVID-19 with both hypoxia and systemic inflammation. METHODS: This randomised, controlled, open-label, platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]), is assessing several possible treatments in patients hospitalised with COVID-19 in the UK. Those trial participants with hypoxia (oxygen saturation <92% on air or requiring oxygen therapy) and evidence of systemic inflammation (C-reactive protein ≥75 mg/L) were eligible for random assignment in a 1:1 ratio to usual standard of care alone versus usual standard of care plus tocilizumab at a dose of 400 mg-800 mg (depending on weight) given intravenously. A second dose could be given 12-24 h later if the patient's condition had not improved. The primary outcome was 28-day mortality, assessed in the intention-to-treat population. The trial is registered with ISRCTN (50189673) and ClinicalTrials.gov (NCT04381936). FINDINGS: Between April 23, 2020, and Jan 24, 2021, 4116 adults of 21 550 patients enrolled into the RECOVERY trial were included in the assessment of tocilizumab, including 3385 (82%) patients receiving systemic corticosteroids. Overall, 621 (31%) of the 2022 patients allocated tocilizumab and 729 (35%) of the 2094 patients allocated to usual care died within 28 days (rate ratio 0·85; 95% CI 0·76-0·94; p=0·0028). Consistent results were seen in all prespecified subgroups of patients, including those receiving systemic corticosteroids. Patients allocated to tocilizumab were more likely to be discharged from hospital within 28 days (57% vs 50%; rate ratio 1·22; 1·12-1·33; p<0·0001). Among those not receiving invasive mechanical ventilation at baseline, patients allocated tocilizumab were less likely to reach the composite endpoint of invasive mechanical ventilation or death (35% vs 42%; risk ratio 0·84; 95% CI 0·77-0·92; p<0·0001). INTERPRETATION: In hospitalised COVID-19 patients with hypoxia and systemic inflammation, tocilizumab improved survival and other clinical outcomes. These benefits were seen regardless of the amount of respiratory support and were additional to the benefits of systemic corticosteroids. FUNDING: UK Research and Innovation (Medical Research Council) and National Institute of Health Research.
背景:在这项研究中,我们旨在评估托珠单抗在伴有低氧血症和全身炎症的 COVID-19 住院成人患者中的疗效。
方法:这是一项随机、对照、开放标签、平台试验(随机评估 COVID-19 治疗[RECOVERY]),正在英国评估 COVID-19 住院患者的几种可能治疗方法。那些有低氧血症(空气氧饱和度<92%或需要氧疗)和全身炎症证据(C 反应蛋白≥75mg/L)的试验参与者,按 1:1 的比例随机分配,接受标准治疗加托珠单抗,剂量为 400mg-800mg(根据体重)静脉注射。如果患者病情没有改善,可以在 12-24 小时后给予第二剂。主要结局为 28 天死亡率,在意向治疗人群中评估。该试验在 ISRCTN(50189673)和 ClinicalTrials.gov(NCT04381936)注册。
结果:2020 年 4 月 23 日至 2021 年 1 月 24 日,共有 21550 名患者中的 4116 名成年人参加了 RECOVERY 试验,其中 3385 名(82%)患者接受了全身皮质激素治疗。总体而言,在接受托珠单抗治疗的 2022 名患者中,有 621 名(31%)和在接受常规治疗的 2094 名患者中,有 729 名(35%)在 28 天内死亡(率比 0.85;95%CI 0.76-0.94;p=0.0028)。在所有预先指定的患者亚组中均观察到一致的结果,包括接受全身皮质激素治疗的患者。接受托珠单抗治疗的患者更有可能在 28 天内出院(57%比 50%;率比 1.22;1.12-1.33;p<0.0001)。在基线时未接受有创机械通气的患者中,接受托珠单抗治疗的患者不太可能达到有创机械通气或死亡的复合终点(35%比 42%;风险比 0.84;95%CI 0.77-0.92;p<0.0001)。
解释:在伴有低氧血症和全身炎症的 COVID-19 住院患者中,托珠单抗改善了生存率和其他临床结局。这些益处与呼吸支持的程度无关,并且是全身皮质激素治疗益处的补充。
经费:英国研究与创新署(医学研究理事会)和英国国家卫生研究院。
Microorganisms. 2025-7-31
Infect Drug Resist. 2025-8-8
Reports (MDPI). 2023-9-22
Circ Genom Precis Med. 2025-8
Lancet Respir Med. 2021-5
N Engl J Med. 2021-4-22
N Engl J Med. 2021-4-22
N Engl J Med. 2021-1-7
Am J Respir Crit Care Med. 2021-1-15